Egenskap
Low blood sugar
Klinisk navn: Hypoglycemia
A decreased concentration of glucose in the blood.
Sammendrag
- Også kalt
- Hypoglycaemia
- Kroppssystem
- Laboratory abnormality
ReferansegenomGRCh38hg38
Posisjoner på gen- og variantsidene følger dette valget i denne nettleseren.
Read the genes linked to Low blood sugar, and the rest of your genome, with one test.
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Få mitt Genome Test222 gener knyttet til Low blood sugar
Endringer i disse genene forårsaker sjeldne tilstander der Low blood sugar forekommer. De fleste med denne egenskapen har ingen av disse tilstandene, og et gen på denne listen sier ingenting om noens eget genom.
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| ABCC8ATP binding cassette subfamily C member 8 | Alltid | I 1 tilstand |
| ALG12ALG12 alpha-1,6-mannosyltransferase | Alltid | I 1 tilstand |
| ALPK3alpha kinase 3 | Alltid | I 1 tilstand |
| ATIC5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase | Alltid | I 1 tilstand |
| ATP5F1DATP synthase F1 subunit delta | Alltid | I 1 tilstand |
| BCS1LBCS1 ubiquinol-cytochrome c reductase complex chaperone | Alltid | I 1 tilstand |
| CA5Acarbonic anhydrase 5A | Alltid | I 1 tilstand |
| COX16cytochrome c oxidase assembly factor COX16 | Alltid | I 1 tilstand |
| CYB561cytochrome b561 | Alltid | I 1 tilstand |
| DMXL2Dmx like 2 | Alltid | I 2 tilstander |
| FARSBphenylalanyl-tRNA synthetase subunit beta | Alltid | I 1 tilstand |
| FBP1fructose-bisphosphatase 1 | Alltid | I 2 tilstander |
| FDXRferredoxin reductase | Alltid | I 1 tilstand |
| GCSHglycine cleavage system protein H | Alltid | I 1 tilstand |
| GH1growth hormone 1 | Alltid | I 1 tilstand |
| GLI2GLI family zinc finger 2 | Alltid | I 2 tilstander |
| GYS1glycogen synthase 1 | Alltid | I 1 tilstand |
| HNF4Ahepatocyte nuclear factor 4 alpha | Alltid | I 1 tilstand |
| HYOU1hypoxia up-regulated 1 | Alltid | I 1 tilstand |
| IARS1isoleucyl-tRNA synthetase 1 | Alltid | I 1 tilstand |
| IARS2isoleucyl-tRNA synthetase 2, mitochondrial | Alltid | I 2 tilstander |
| IRF4interferon regulatory factor 4 | Alltid | I 1 tilstand |
| KDM6Blysine demethylase 6B | Alltid | I 1 tilstand |
| MICOS13mitochondrial contact site and cristae organizing system subunit 13 | Alltid | I 1 tilstand |
| MMABmetabolism of cobalamin associated B | Alltid | I 1 tilstand |
| MMUTmethylmalonyl-CoA mutase | Alltid | I 1 tilstand |
| MRAPmelanocortin 2 receptor accessory protein | Alltid | I 1 tilstand |
| MRPS2mitochondrial ribosomal protein S2 | Alltid | I 1 tilstand |
| MRPS28mitochondrial ribosomal protein S28 | Alltid | I 1 tilstand |
| MRPS7mitochondrial ribosomal protein S7 | Alltid | I 1 tilstand |
| NSD1nuclear receptor binding SET domain protein 1 | Alltid | I 1 tilstand |
| ODC1ornithine decarboxylase 1 | Alltid | I 1 tilstand |
| OTX2orthodenticle homeobox 2 | Alltid | I 3 tilstander |
| PCK1phosphoenolpyruvate carboxykinase 1 | Alltid | I 1 tilstand |
| PET100PET100 cytochrome c oxidase chaperone | Alltid | I 1 tilstand |
| PEX1peroxisomal biogenesis factor 1 | Alltid | I 1 tilstand |
| PGM1phosphoglucomutase 1 | Alltid | I 1 tilstand |
| PHKA1phosphorylase kinase regulatory subunit alpha 1 | Alltid | I 1 tilstand |
| PTBP1polypyrimidine tract binding protein 1 | Alltid | I 1 tilstand |
| RPL17ribosomal protein L17 | Alltid | I 1 tilstand |
Vis 182 gener til
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| RRAGCRas related GTP binding C | Alltid | I 1 tilstand |
| SCO1synthesis of cytochrome C oxidase 1 | Alltid | I 1 tilstand |
| SLC25A36solute carrier family 25 member 36 | Alltid | I 1 tilstand |
| SLC37A4solute carrier family 37 member 4 | Alltid | I 3 tilstander |
| SUCLG1succinate-CoA ligase GDP/ADP-forming subunit alpha | Alltid | I 2 tilstander |
| TEFMtranscription elongation factor, mitochondrial | Alltid | I 1 tilstand |
| TFAMtranscription factor A, mitochondrial | Alltid | I 1 tilstand |
| UQCC3ubiquinol-cytochrome c reductase complex assembly factor 3 | Alltid | I 1 tilstand |
| UQCRBubiquinol-cytochrome c reductase binding protein | Alltid | I 1 tilstand |
| UQCRC2ubiquinol-cytochrome c reductase core protein 2 | Alltid | I 1 tilstand |
| UQCRHubiquinol-cytochrome c reductase hinge protein | Alltid | I 1 tilstand |
| WARS2tryptophanyl tRNA synthetase 2, mitochondrial | Alltid | I 1 tilstand |
| AGLamylo-alpha-1,6-glucosidase and 4-alpha-glucanotransferase | Svært ofte (80–99 %) | I 2 tilstander |
| CPT1Acarnitine palmitoyltransferase 1A | Svært ofte (80–99 %) | I 1 tilstand |
| FOXRED1FAD dependent oxidoreductase domain containing 1 | Svært ofte (80–99 %) | I 2 tilstander |
| GHSRgrowth hormone secretagogue receptor | Svært ofte (80–99 %) | I 1 tilstand |
| HADHAhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha | Svært ofte (80–99 %) | I 2 tilstander |
| HMGCL3-hydroxy-3-methylglutaryl-CoA lyase | Svært ofte (80–99 %) | I 1 tilstand |
| HMGCS23-hydroxy-3-methylglutaryl-CoA synthase 2 | Svært ofte (80–99 %) | I 2 tilstander |
| INSRinsulin receptor | Svært ofte (80–99 %) | I 2 tilstander |
| MCCC1methylcrotonyl-CoA carboxylase subunit 1 | Svært ofte (80–99 %) | I 2 tilstander |
| MCCC2methylcrotonyl-CoA carboxylase subunit 2 | Svært ofte (80–99 %) | I 2 tilstander |
| MT-ND1mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 | Svært ofte (80–99 %) | I 1 tilstand |
| MT-ND2mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 | Svært ofte (80–99 %) | I 1 tilstand |
| MT-ND3mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFA1NADH:ubiquinone oxidoreductase subunit A1 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFA11NADH:ubiquinone oxidoreductase subunit A11 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFA6NADH:ubiquinone oxidoreductase subunit A6 | Svært ofte (80–99 %) | I 2 tilstander |
| NDUFA9NADH:ubiquinone oxidoreductase subunit A9 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFAF1NADH:ubiquinone oxidoreductase complex assembly factor 1 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFAF2NADH:ubiquinone oxidoreductase complex assembly factor 2 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFAF3NADH:ubiquinone oxidoreductase complex assembly factor 3 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFAF4NADH:ubiquinone oxidoreductase complex assembly factor 4 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFAF5NADH:ubiquinone oxidoreductase complex assembly factor 5 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFAF8NADH:ubiquinone oxidoreductase complex assembly factor 8 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFB10NADH:ubiquinone oxidoreductase subunit B10 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFB11NADH:ubiquinone oxidoreductase subunit B11 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFB3NADH:ubiquinone oxidoreductase subunit B3 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFB9NADH:ubiquinone oxidoreductase subunit B9 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFS1NADH:ubiquinone oxidoreductase core subunit S1 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFS2NADH:ubiquinone oxidoreductase core subunit S2 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFS3NADH:ubiquinone oxidoreductase core subunit S3 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFS4NADH:ubiquinone oxidoreductase subunit S4 | Svært ofte (80–99 %) | I 2 tilstander |
| NDUFS6NADH:ubiquinone oxidoreductase subunit S6 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFS7NADH:ubiquinone oxidoreductase core subunit S7 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFS8NADH:ubiquinone oxidoreductase core subunit S8 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFV1NADH:ubiquinone oxidoreductase core subunit V1 | Svært ofte (80–99 %) | I 1 tilstand |
| NDUFV2NADH:ubiquinone oxidoreductase core subunit V2 | Svært ofte (80–99 %) | I 1 tilstand |
| NUBPLNUBP iron-sulfur cluster assembly factor, mitochondrial | Svært ofte (80–99 %) | I 1 tilstand |
| OTCornithine transcarbamylase | Svært ofte (80–99 %) | I 1 tilstand |
| PCCApropionyl-CoA carboxylase subunit alpha | Svært ofte (80–99 %) | I 2 tilstander |
| PCCBpropionyl-CoA carboxylase subunit beta | Svært ofte (80–99 %) | I 2 tilstander |
| TIMMDC1translocase of inner mitochondrial membrane domain containing 1 | Svært ofte (80–99 %) | I 1 tilstand |
| TMEM126Btransmembrane protein 126B | Svært ofte (80–99 %) | I 1 tilstand |
| AAASaladin WD repeat nucleoporin | Ofte (30–79 %) | I 1 tilstand |
| AKT2AKT serine/threonine kinase 2 | Ofte (30–79 %) | I 1 tilstand |
| ASXL2ASXL transcriptional regulator 2 | Ofte (30–79 %) | I 1 tilstand |
| CACNA1Ccalcium voltage-gated channel subunit alpha1 C | Ofte (30–79 %) | I 1 tilstand |
| CDONcell adhesion associated, oncogene regulated | Ofte (30–79 %) | I 1 tilstand |
| COG7component of oligomeric golgi complex 7 | Ofte (30–79 %) | I 1 tilstand |
| COX11cytochrome c oxidase copper chaperone COX11 | Ofte (30–79 %) | I 1 tilstand |
| CPT2carnitine palmitoyltransferase 2 | Ofte (30–79 %) | I 1 tilstand |
| CYC1cytochrome c1 | Ofte (30–79 %) | I 1 tilstand |
| DAP3death associated protein 3 | Ofte (30–79 %) | I 1 tilstand |
| DBHdopamine beta-hydroxylase | Ofte (30–79 %) | I 1 tilstand |
| DIS3L2DIS3 like 3'-5' exoribonuclease 2 | Ofte (30–79 %) | I 1 tilstand |
| DLDdihydrolipoamide dehydrogenase | Ofte (30–79 %) | I 2 tilstander |
| FAHfumarylacetoacetate hydrolase | Ofte (30–79 %) | I 1 tilstand |
| FOXA2forkhead box A2 | Ofte (30–79 %) | I 1 tilstand |
| FUT8fucosyltransferase 8 | Ofte (30–79 %) | I 1 tilstand |
| GHRgrowth hormone receptor | Ofte (30–79 %) | I 2 tilstander |
| GLYCTKglycerate kinase | Ofte (30–79 %) | I 1 tilstand |
| GMPPAGDP-mannose pyrophosphorylase A | Ofte (30–79 %) | I 1 tilstand |
| GPC3glypican 3 | Ofte (30–79 %) | I 1 tilstand |
| GPC4glypican 4 | Ofte (30–79 %) | I 1 tilstand |
| GPR161G protein-coupled receptor 161 | Ofte (30–79 %) | I 1 tilstand |
| HADHBhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta | Ofte (30–79 %) | I 1 tilstand |
| HESX1HESX homeobox 1 | Ofte (30–79 %) | I 3 tilstander |
| HSD17B10hydroxysteroid 17-beta dehydrogenase 10 | Ofte (30–79 %) | I 2 tilstander |
| LHX4LIM homeobox 4 | Ofte (30–79 %) | I 4 tilstander |
| LRPPRCleucine rich pentatricopeptide repeat containing | Ofte (30–79 %) | I 1 tilstand |
| MLYCDmalonyl-CoA decarboxylase | Ofte (30–79 %) | I 2 tilstander |
| MPV17mitochondrial inner membrane protein MPV17 | Ofte (30–79 %) | I 1 tilstand |
| MTO1mitochondrial tRNA translation optimization 1 | Ofte (30–79 %) | I 2 tilstander |
| NFS1NFS1 cysteine desulfurase | Ofte (30–79 %) | I 1 tilstand |
| NR1H4nuclear receptor subfamily 1 group H member 4 | Ofte (30–79 %) | I 1 tilstand |
| PHKA2phosphorylase kinase regulatory subunit alpha 2 | Ofte (30–79 %) | I 2 tilstander |
| PHKBphosphorylase kinase regulatory subunit beta | Ofte (30–79 %) | I 1 tilstand |
| PHKG2phosphorylase kinase catalytic subunit gamma 2 | Ofte (30–79 %) | I 2 tilstander |
| PNPOpyridoxamine 5'-phosphate oxidase | Ofte (30–79 %) | I 2 tilstander |
| PORcytochrome p450 oxidoreductase | Ofte (30–79 %) | I 1 tilstand |
| POU1F1POU class 1 homeobox 1 | Ofte (30–79 %) | I 2 tilstander |
| PPP1R15Bprotein phosphatase 1 regulatory subunit 15B | Ofte (30–79 %) | I 1 tilstand |
| PROKR2prokineticin receptor 2 | Ofte (30–79 %) | I 1 tilstand |
| PROP1PROP paired-like homeobox 1 | Ofte (30–79 %) | I 3 tilstander |
| PYGLglycogen phosphorylase L | Ofte (30–79 %) | I 2 tilstander |
| RNF125ring finger protein 125 | Ofte (30–79 %) | I 1 tilstand |
| ROBO1roundabout guidance receptor 1 | Ofte (30–79 %) | I 1 tilstand |
| SOX3SRY-box transcription factor 3 | Ofte (30–79 %) | I 1 tilstand |
| STIM1stromal interaction molecule 1 | Ofte (30–79 %) | I 1 tilstand |
| TANGO2transport and golgi organization 2 homolog | Ofte (30–79 %) | I 2 tilstander |
| TFE3transcription factor binding to IGHM enhancer 3 | Ofte (30–79 %) | I 1 tilstand |
| TRAPPC11trafficking protein particle complex subunit 11 | Ofte (30–79 %) | I 1 tilstand |
| TRMT10AtRNA methyltransferase 10A | Ofte (30–79 %) | I 1 tilstand |
| WDR11WD repeat domain 11 | Ofte (30–79 %) | I 1 tilstand |
| YARS1tyrosyl-tRNA synthetase 1 | Ofte (30–79 %) | I 1 tilstand |
| ACADMacyl-CoA dehydrogenase medium chain | Noen ganger (5–29 %) | I 2 tilstander |
| ACAT1acetyl-CoA acetyltransferase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| ACSF3acyl-CoA synthetase family member 3 | Noen ganger (5–29 %) | I 1 tilstand |
| ATP7AATPase copper transporting alpha | Noen ganger (5–29 %) | I 1 tilstand |
| AUHAU RNA binding methylglutaconyl-CoA hydratase | Noen ganger (5–29 %) | I 1 tilstand |
| CAMKMTcalmodulin-lysine N-methyltransferase | Noen ganger (5–29 %) | I 1 tilstand |
| CDKN1Ccyclin dependent kinase inhibitor 1C | Noen ganger (5–29 %) | I 1 tilstand |
| COG8component of oligomeric golgi complex 8 | Noen ganger (5–29 %) | I 1 tilstand |
| CTDP1CTD phosphatase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| DDCdopa decarboxylase | Noen ganger (5–29 %) | I 1 tilstand |
| FBXO22F-box protein 22 | Noen ganger (5–29 %) | I 1 tilstand |
| GALTgalactose-1-phosphate uridylyltransferase | Noen ganger (5–29 %) | I 1 tilstand |
| GATBglutamyl-tRNA amidotransferase subunit B | Noen ganger (5–29 %) | I 1 tilstand |
| GATCglutamyl-tRNA amidotransferase subunit C | Noen ganger (5–29 %) | I 1 tilstand |
| GFM1G elongation factor mitochondrial 1 | Noen ganger (5–29 %) | I 1 tilstand |
| GJA1gap junction protein alpha 1 | Noen ganger (5–29 %) | I 1 tilstand |
| H19H19 imprinted maternally expressed transcript | Noen ganger (5–29 %) | I 1 tilstand |
| HMGA2high mobility group AT-hook 2 | Noen ganger (5–29 %) | I 1 tilstand |
| IGF1insulin like growth factor 1 | Noen ganger (5–29 %) | I 1 tilstand |
| IGF2insulin like growth factor 2 | Noen ganger (5–29 %) | I 2 tilstander |
| KDM6Alysine demethylase 6A | Noen ganger (5–29 %) | I 1 tilstand |
| KMT2Dlysine methyltransferase 2D | Noen ganger (5–29 %) | I 1 tilstand |
| LHX3LIM homeobox 3 | Noen ganger (5–29 %) | I 1 tilstand |
| MMACHCmetabolism of cobalamin associated C | Noen ganger (5–29 %) | I 1 tilstand |
| NR3C1nuclear receptor subfamily 3 group C member 1 | Noen ganger (5–29 %) | I 2 tilstander |
| OPLAH5-oxoprolinase, ATP-hydrolysing | Noen ganger (5–29 %) | I 1 tilstand |
| PCpyruvate carboxylase | Noen ganger (5–29 %) | I 1 tilstand |
| PLAG1PLAG1 zinc finger | Noen ganger (5–29 %) | I 1 tilstand |
| PPM1Bprotein phosphatase, Mg2+/Mn2+ dependent 1B | Noen ganger (5–29 %) | I 1 tilstand |
| PPP2R5Dprotein phosphatase 2 regulatory subunit B'delta | Noen ganger (5–29 %) | I 2 tilstander |
| PREPLprolyl endopeptidase like | Noen ganger (5–29 %) | I 1 tilstand |
| PTENphosphatase and tensin homolog | Noen ganger (5–29 %) | I 1 tilstand |
| QRSL1glutaminyl-tRNA amidotransferase subunit QRSL1 | Noen ganger (5–29 %) | I 1 tilstand |
| SLC3A1solute carrier family 3 member 1 | Noen ganger (5–29 %) | I 1 tilstand |
| SNIP1Smad nuclear interacting protein 1 | Noen ganger (5–29 %) | I 1 tilstand |
| TRPM3transient receptor potential cation channel subfamily M member 3 | Noen ganger (5–29 %) | I 1 tilstand |
| ALDH7A1aldehyde dehydrogenase 7 family member A1 | Sjelden (1–4%) | I 1 tilstand |
| EHHADHenoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase | Sjelden (1–4%) | I 1 tilstand |
| FHfumarate hydratase | Sjelden (1–4%) | I 1 tilstand |
| GALK1galactokinase 1 | Sjelden (1–4%) | I 1 tilstand |
| GATMglycine amidinotransferase | Sjelden (1–4%) | I 1 tilstand |
| MT-CYBmitochondrially encoded cytochrome b | Sjelden (1–4%) | I 1 tilstand |
| NAB2NGFI-A binding protein 2 | Sjelden (1–4%) | I 1 tilstand |
| NDUFAF6NADH:ubiquinone oxidoreductase complex assembly factor 6 | Sjelden (1–4%) | I 1 tilstand |
| PLPBPpyridoxal phosphate binding protein | Sjelden (1–4%) | I 1 tilstand |
| SLC34A1solute carrier family 34 member 1 | Sjelden (1–4%) | I 1 tilstand |
| STAT6signal transducer and activator of transcription 6 | Sjelden (1–4%) | I 1 tilstand |
| ACAD9acyl-CoA dehydrogenase family member 9 | Ikke registrert | I 1 tilstand |
| ACADSBacyl-CoA dehydrogenase short/branched chain | Ikke registrert | I 1 tilstand |
| ALDOBaldolase, fructose-bisphosphate B | Ikke registrert | I 1 tilstand |
| BCKDHAbranched chain keto acid dehydrogenase E1 subunit alpha | Ikke registrert | I 1 tilstand |
| CYP21A2cytochrome P450 family 21 subfamily A member 2 | Ikke registrert | I 1 tilstand |
| DGUOKdeoxyguanosine kinase | Ikke registrert | I 1 tilstand |
| EIF2S3eukaryotic translation initiation factor 2 subunit gamma | Ikke registrert | I 1 tilstand |
| ETFAelectron transfer flavoprotein subunit alpha | Ikke registrert | I 1 tilstand |
| ETFBelectron transfer flavoprotein subunit beta | Ikke registrert | I 1 tilstand |
| ETFDHelectron transfer flavoprotein dehydrogenase | Ikke registrert | I 1 tilstand |
| G6PC1glucose-6-phosphatase catalytic subunit 1 | Ikke registrert | I 1 tilstand |
| GCDHglutaryl-CoA dehydrogenase | Ikke registrert | I 1 tilstand |
| GKglycerol kinase | Ikke registrert | I 1 tilstand |
| HRASHRas proto-oncogene, GTPase | Ikke registrert | I 1 tilstand |
| KCNJ11potassium inwardly rectifying channel subfamily J member 11 | Ikke registrert | I 1 tilstand |
| MEN1menin 1 | Ikke registrert | I 1 tilstand |
| MPC1mitochondrial pyruvate carrier 1 | Ikke registrert | I 1 tilstand |
| MTORmechanistic target of rapamycin kinase | Ikke registrert | I 1 tilstand |
| NBASNBAS subunit of NRZ tethering complex | Ikke registrert | I 1 tilstand |
| NFKB2nuclear factor kappa B subunit 2 | Ikke registrert | I 1 tilstand |
| NNTnicotinamide nucleotide transhydrogenase | Ikke registrert | I 1 tilstand |
| PCK2phosphoenolpyruvate carboxykinase 2, mitochondrial | Ikke registrert | I 1 tilstand |
| PTF1Apancreas associated transcription factor 1a | Ikke registrert | I 1 tilstand |
| SAMD9sterile alpha motif domain containing 9 | Ikke registrert | I 1 tilstand |
| SERAC1serine active site containing 1 | Ikke registrert | I 1 tilstand |
| SGPL1sphingosine-1-phosphate lyase 1 | Ikke registrert | I 1 tilstand |
| SLC16A1solute carrier family 16 member 1 | Ikke registrert | I 1 tilstand |
| SLC25A20solute carrier family 25 member 20 | Ikke registrert | I 1 tilstand |
| SLC52A1solute carrier family 52 member 1 | Ikke registrert | I 1 tilstand |
Hvor ofte dette forekommer hos personer med en av genets tilstander, oppgitt som den hyppigste forekomsten blant dem, slik Human Phenotype Ontology registrerer den. Disse sidene beskriver egenskaper og forskningen bak dem. De er ikke en diagnose, og om symptomer bør du spørre lege eller genetisk rådgiver.
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Slik er informasjonen samlet
- Human Phenotype Ontology, versjon 2026-09-01: egenskapen, navnene på den, definisjonen og genene som er knyttet til den. Les mer på hpo.jax.org.
- Datautgave 2026.10.16-c6eea6bf.
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Fra 449 $Gratis frakt · Resultater på 6–8 uker